메뉴 건너뛰기




Volumn 287, Issue 32, 2012, Pages 27020-27025

Chemical synthesis of circular proteins

Author keywords

[No Author keywords available]

Indexed keywords

CAPTURE REACTION; CHEMICAL LIGATION; CHEMICAL SYNTHESIS; CHEMOSELECTIVE; CIRCULAR PROTEINS; EXTRA DIMENSIONS; KEY ELEMENTS; MACRO-CYCLIZATION; SIDE-CHAINS;

EID: 84864568542     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.R111.323568     Document Type: Short Survey
Times cited : (59)

References (61)
  • 1
    • 73749087526 scopus 로고    scopus 로고
    • Cyclotides as templates in drug design
    • Henriques, S. T., and Craik, D. J. (2010) Cyclotides as templates in drug design. Drug Discov. Today 15, 57-64
    • (2010) Drug Discov. Today , vol.15 , pp. 57-64
    • Henriques, S.T.1    Craik, D.J.2
  • 2
    • 33645116726 scopus 로고    scopus 로고
    • Chemoenzymatic and template-directed synthesis of bioactive macrocyclic peptides
    • Grünewald, J., and Marahiel, M. A. (2006) Chemoenzymatic and template-directed synthesis of bioactive macrocyclic peptides. Microbiol. Mol. Biol. Rev. 70, 121-146
    • (2006) Microbiol. Mol. Biol. Rev. , vol.70 , pp. 121-146
    • Grünewald, J.1    Marahiel, M.A.2
  • 4
    • 0015723952 scopus 로고
    • On the effect of a polypeptide isolated from "Kalata-Kalata" (Oldenlandia affinis DC) on the estrogen-dominated uterus
    • Gran, L. (1973) On the effect of a polypeptide isolated from "Kalata-Kalata" (Oldenlandia affinis DC) on the estrogen-dominated uterus. Acta Pharmacol. Toxicol. 33, 400-408
    • (1973) Acta Pharmacol. Toxicol. , vol.33 , pp. 400-408
    • Gran, L.1
  • 5
    • 0038492655 scopus 로고    scopus 로고
    • Structures of naturally occurring circular proteins from bacteria
    • DOI 10.1128/JB.185.14.4011-4021.2003
    • Craik, D. J., Daly, N. L., Saska, I., Trabi, M., and Rosengren, K. J. (2003) Structures of naturally occurring circular proteins from bacteria. J. Bacteriol. 185, 4011-4021 (Pubitemid 36835239)
    • (2003) Journal of Bacteriology , vol.185 , Issue.14 , pp. 4011-4021
    • Craik, D.J.1    Daly, N.L.2    Saska, I.3    Trabi, M.4    Rosengren, K.J.5
  • 6
    • 0033569410 scopus 로고    scopus 로고
    • A cyclic antimicrobial peptide produced in primate leukocytes by the ligation of two truncated αins
    • Tang, Y. Q., Yuan, J., Ösapay, G., Ösapay, K., Tran, D., Miller, C. J., Ouellette, A. J., and Selsted, M. E. (1999) A cyclic antimicrobial peptide produced in primate leukocytes by the ligation of two truncated αins. Science 286, 498-502
    • (1999) Science , vol.286 , pp. 498-502
    • Tang, Y.Q.1    Yuan, J.2    Ösapay, G.3    Ösapay, K.4    Tran, D.5    Miller, C.J.6    Ouellette, A.J.7    Selsted, M.E.8
  • 7
    • 0017157814 scopus 로고
    • Biological effects of cyclosporin A: A new antilymphocytic agent
    • Borel, J. F., Feurer, C., Gubler, H. U., and Stähelin, H. (1976) Biological effects of cyclosporin A: a new antilymphocytic agent. Agents Actions 6, 468-475
    • (1976) Agents Actions , vol.6 , pp. 468-475
    • Borel, J.F.1    Feurer, C.2    Gubler, H.U.3    Stähelin, H.4
  • 8
    • 0030808964 scopus 로고    scopus 로고
    • Synthesis of large cyclic cystine-knot peptide by orthogonal coupling strategy using unprotected peptide precursor
    • DOI 10.1016/S0040-4039(97)01271-9, PII S0040403997012719
    • Tam, J. P., and Lu, Y. A. (1997) Synthesis of large cyclic cystine knot peptide by orthogonal coupling strategy using unprotected peptide precursors. Tetrahedron Lett. 38, 5599-5602 (Pubitemid 27321132)
    • (1997) Tetrahedron Letters , vol.38 , Issue.32 , pp. 5599-5602
    • Tam, J.P.1    Lu, Y.-A.2
  • 9
    • 0031822610 scopus 로고    scopus 로고
    • A biomimetic strategy in the synthesis and fragmentation of cyclic protein
    • Tam, J. P., and Lu, Y. A. (1998) A biomimetic strategy in the synthesis and fragmentation of cyclic protein. Protein Sci. 7, 1583-1592 (Pubitemid 28331278)
    • (1998) Protein Science , vol.7 , Issue.7 , pp. 1583-1592
    • Tam, J.P.1    Lu, Y.I.-A.N.2
  • 10
    • 79958826757 scopus 로고    scopus 로고
    • The chemistry of cyclotides
    • Craik, D. J., and Conibear, A. C. (2011) The chemistry of cyclotides. J. Org. Chem. 76, 4805-4817
    • (2011) J. Org. Chem. , vol.76 , pp. 4805-4817
    • Craik, D.J.1    Conibear, A.C.2
  • 11
    • 57749121492 scopus 로고    scopus 로고
    • Chemoselective ligation and modification strategies for peptides and proteins
    • Hackenberger, C. P., and Schwarzer, D. (2008) Chemoselective ligation and modification strategies for peptides and proteins. Angew. Chem. Int. Ed. Engl. 47, 10030-10074
    • (2008) Angew. Chem. Int. Ed. Engl. , vol.47 , pp. 10030-10074
    • Hackenberger, C.P.1    Schwarzer, D.2
  • 12
    • 79959580534 scopus 로고    scopus 로고
    • Contemporary strategies for peptide macrocyclization
    • White, C. J., and Yudin, A. K. (2011) Contemporary strategies for peptide macrocyclization. Nat. Chem. 3, 509-524
    • (2011) Nat. Chem. , vol.3 , pp. 509-524
    • White, C.J.1    Yudin, A.K.2
  • 13
    • 0033500546 scopus 로고    scopus 로고
    • Orthogonal ligation strategies for peptide and protein
    • DOI 10.1002/(SICI)1097-0282(1999)51:5<311::AID-BIP2>3.0.CO;2-A
    • Tam, J. P., Yu, Q., and Miao, Z. (1999) Orthogonal ligation strategies for peptide and protein. Biopolymers 51, 311-332 (Pubitemid 30117292)
    • (1999) Biopolymers - Peptide Science Section , vol.51 , Issue.5 , pp. 311-332
    • Tam, J.P.1    Yu, Q.2    Miao, Z.3
  • 14
    • 84985687610 scopus 로고
    • The amine capture strategy for peptide bond formation-an outline of progress
    • Kemp, D. S. (1981) The amine capture strategy for peptide bond formation-an outline of progress. Biopolymers 20, 1793-1804
    • (1981) Biopolymers , vol.20 , pp. 1793-1804
    • Kemp, D.S.1
  • 15
    • 12044253737 scopus 로고
    • Chemical ligation approach to form a peptide bond between two unprotected peptide segments. Concept and model study
    • Liu, C. F., and Tam, J. P. (1994) Chemical ligation approach to form a peptide bond between two unprotected peptide segments. Concept and model study. J. Am. Chem. Soc 116, 4149-4153
    • (1994) J. Am. Chem. Soc , vol.116 , pp. 4149-4153
    • Liu, C.F.1    Tam, J.P.2
  • 16
    • 0028223433 scopus 로고
    • Peptide segment ligation strategy without use of protecting groups
    • Liu, C. F., and Tam, J. P. (1994) Peptide segment ligation strategy without use of protecting groups. Proc. Natl. Acad. Sci. U.S.A. 91, 6584-6588
    • (1994) Proc. Natl. Acad. Sci. U.S.A. , vol.91 , pp. 6584-6588
    • Liu, C.F.1    Tam, J.P.2
  • 17
    • 0027944205 scopus 로고
    • Synthesis of proteins by native chemical ligation
    • Dawson, P. E., Muir, T. W., Clark-Lewis, I., and Kent, S. B. (1994) Synthesis of proteins by native chemical ligation. Science 266, 776-779 (Pubitemid 24359280)
    • (1994) Science , vol.266 , Issue.5186 , pp. 776-779
    • Dawson, P.E.1    Muir, T.W.2    Clark-Lewis, I.3    Kent, S.B.H.4
  • 20
    • 0031013619 scopus 로고    scopus 로고
    • Orthogonal coupling of unprotected peptide segments through histidyl amino terminus
    • DOI 10.1016/S0040-4039(96)02260-5, PII S0040403996022605
    • Zhang, L., and Tam, J. P. (1997) Orthogonal coupling of unprotected peptide segments through histidyl amino terminus. Tetrahedron Lett. 38, 3-6 (Pubitemid 27018825)
    • (1997) Tetrahedron Letters , vol.38 , Issue.1 , pp. 3-6
    • Zhang, L.1    Tam, J.P.2
  • 21
    • 0027753790 scopus 로고
    • In vitro protein splicing of purified precursor and the identification of a branched intermediate
    • DOI 10.1016/0092-8674(93)90623-X
    • Xu, M. Q., Southworth, M. W., Mersha, F. B., Hornstra, L. J., and Perler, F. B. (1993) In vitro protein splicing of purified precursor and the identification of a branched intermediate. Cell 75, 1371-1377 (Pubitemid 24021911)
    • (1993) Cell , vol.75 , Issue.7 , pp. 1371-1377
    • Xu, M.-Q.1    Southworth, M.W.2    Mersha, F.B.3    Hornstra, L.J.4    Perler, F.B.5
  • 22
    • 0032568924 scopus 로고    scopus 로고
    • Expressed protein ligation, a novel method for studying protein-protein interactions in transcription
    • DOI 10.1074/jbc.273.26.16205
    • Severinov, K., and Muir, T. W. (1998) Expressed protein ligation, a novel method for studying protein-protein interactions in transcription. J. Biol. Chem. 273, 16205-16209 (Pubitemid 28311394)
    • (1998) Journal of Biological Chemistry , vol.273 , Issue.26 , pp. 16205-16209
    • Severinov, K.1    Muir, T.W.2
  • 23
    • 77957758860 scopus 로고    scopus 로고
    • Biological applications of protein splicing
    • Vila-Perelló, M., and Muir, T. W. (2010) Biological applications of protein splicing. Cell 143, 191-200
    • (2010) Cell , vol.143 , pp. 191-200
    • Vila-Perelló, M.1    Muir, T.W.2
  • 25
    • 67649592405 scopus 로고    scopus 로고
    • Conotoxins: Natural product drug leads
    • Halai, R., and Craik, D. J. (2009) Conotoxins: natural product drug leads. Nat. Prod. Rep. 26, 526-536
    • (2009) Nat. Prod. Rep. , vol.26 , pp. 526-536
    • Halai, R.1    Craik, D.J.2
  • 27
    • 0033549108 scopus 로고    scopus 로고
    • Thia-zip reaction for synthesis of large cyclic peptides: Mechanisms and applications
    • Tam, J. P., Lu, Y. A., and Yu, Q. (1999) Thia-zip reaction for synthesis of large cyclic peptides: mechanisms and applications. J. Am. Chem. Soc. 121, 4316-4324
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 4316-4324
    • Tam, J.P.1    Lu, Y.A.2    Yu, Q.3
  • 28
    • 0030913561 scopus 로고    scopus 로고
    • Metal ion-assisted peptide cyclization
    • DOI 10.1016/S0040-4039(97)00935-0, PII S0040403997009350
    • Zhang, L., and Tam, J. P. (1997) Metal ion-assisted peptide cyclization. Tetrahedron Lett. 38, 4375-4378 (Pubitemid 27263399)
    • (1997) Tetrahedron Letters , vol.38 , Issue.25 , pp. 4375-4378
    • Zhang, L.1    Tam, J.P.2
  • 29
    • 38149104557 scopus 로고    scopus 로고
    • Ultra-stable peptide scaffolds for protein engineering-synthesis and folding of the circular cystine knotted cyclotide cycloviolacin O2
    • Aboye, T. L., Clark, R. J., Craik, D. J., and Göransson, U. (2008) Ultra-stable peptide scaffolds for protein engineering-synthesis and folding of the circular cystine knotted cyclotide cycloviolacin O2. ChemBioChem 9, 103-113
    • (2008) ChemBioChem , vol.9 , pp. 103-113
    • Aboye, T.L.1    Clark, R.J.2    Craik, D.J.3    Göransson, U.4
  • 30
    • 80051775850 scopus 로고    scopus 로고
    • Optimal oxidative folding of the novel antimicrobial cyclotide from Hedyotis biflora requires high alcohol concentrations
    • Wong, C. T., Taichi, M., Nishio, H., Nishiuchi, Y., and Tam, J. P. (2011) Optimal oxidative folding of the novel antimicrobial cyclotide from Hedyotis biflora requires high alcohol concentrations. Biochemistry 50, 7275-7283
    • (2011) Biochemistry , vol.50 , pp. 7275-7283
    • Wong, C.T.1    Taichi, M.2    Nishio, H.3    Nishiuchi, Y.4    Tam, J.P.5
  • 31
    • 80054689774 scopus 로고    scopus 로고
    • Identification and characterization of a new family of cell-penetrating peptides: Cyclic cell-penetrating peptides
    • Cascales, L., Henriques, S. T., Kerr, M. C., Huang, Y. H., Sweet, M. J., Daly, N. L., and Craik, D. J. (2011) Identification and characterization of a new family of cell-penetrating peptides: cyclic cell-penetrating peptides. J. Biol. Chem. 286, 36932-36943
    • (2011) J. Biol. Chem. , vol.286 , pp. 36932-36943
    • Cascales, L.1    Henriques, S.T.2    Kerr, M.C.3    Huang, Y.H.4    Sweet, M.J.5    Daly, N.L.6    Craik, D.J.7
  • 33
    • 0033575092 scopus 로고    scopus 로고
    • Biosynthesis of a head-to-tail cyclized protein with improved biological activity
    • DOI 10.1021/ja990929n
    • Camarero, J. A., and Muir, T. W. (1999) Biosynthesis of a head-to-tail cyclized protein with improved biological activity. J. Am. Chem. Soc. 121, 5597-5598 (Pubitemid 29292991)
    • (1999) Journal of the American Chemical Society , vol.121 , Issue.23 , pp. 5597-5598
    • Camarero, J.A.1    Muir, T.W.2
  • 34
    • 0034635459 scopus 로고    scopus 로고
    • Engineered salt-insensitive α-defensins with end-to-end circularized structures
    • DOI 10.1074/jbc.275.6.3943
    • Yu, Q., Lehrer, R. I., and Tam, J. P. (2000) Engineered salt-insensitive α-defensins with end-to-end circularized structures. J. Biol. Chem. 275, 3943-3949 (Pubitemid 30094620)
    • (2000) Journal of Biological Chemistry , vol.275 , Issue.6 , pp. 3943-3949
    • Yu, Q.1    Lehrer, R.I.2    Tam, J.P.3
  • 35
    • 0032189519 scopus 로고    scopus 로고
    • Methionine ligation strategy in the biomimetic synthesis of parathyroid hormones
    • Tam, J. P., and Yu, Q. (1998) Methionine ligation strategy in the biomimetic synthesis of parathyroid hormones. Biopolymers 46, 319-327
    • (1998) Biopolymers , vol.46 , pp. 319-327
    • Tam, J.P.1    Yu, Q.2
  • 37
    • 0041783935 scopus 로고    scopus 로고
    • Native chemical ligation with aspartic and glutamic acids as C-terminal residues: Scope and limitations
    • Villain, M., Gaertner, H., and Botti, P. (2003) Native chemical ligation with aspartic and glutamic acids as C-terminal residues: scope and limitations. Eur. J. Org. Chem. 2003, 3267-3272
    • (2003) Eur. J. Org. Chem. , vol.2003 , pp. 3267-3272
    • Villain, M.1    Gaertner, H.2    Botti, P.3
  • 38
    • 0035977638 scopus 로고    scopus 로고
    • Synthesis of peptides and proteins without cysteine residues by native chemical ligation combined with desulfurization
    • DOI 10.1021/ja003265m
    • Yan, L. Z., and Dawson, P. E. (2001) Synthesis of peptides and proteins without cysteine residues by native chemical ligation combined with desulfurization. J. Am. Chem. Soc. 123, 526-533 (Pubitemid 32105995)
    • (2001) Journal of the American Chemical Society , vol.123 , Issue.4 , pp. 526-533
    • Yan, L.Z.1    Dawson, P.E.2
  • 39
    • 37349094422 scopus 로고    scopus 로고
    • Free-radical-based, specific desulfurization of cysteine: A powerful advance in the synthesis of polypeptides and glycopolypeptides
    • DOI 10.1002/anie.200704195
    • Wan, Q., and Danishefsky, S. J. (2007) Free radical-based specific desulfurization of cysteine: a powerful advance in the synthesis of polypeptides and glycopolypeptides. Angew. Chem. Int. Ed. Engl. 46, 9248-9252 (Pubitemid 350292152)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.48 , pp. 9248-9252
    • Wan, Q.1    Danishefsky, S.J.2
  • 40
    • 34548153495 scopus 로고    scopus 로고
    • Native chemical ligation at phenylalanine
    • DOI 10.1021/ja072804l
    • Crich, D., and Banerjee, A. (2007) Native chemical ligation at phenylalanine. J. Am. Chem. Soc. 129, 10064-10065 (Pubitemid 47312928)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.33 , pp. 10064-10065
    • Crich, D.1    Banerjee, A.2
  • 42
    • 54249149331 scopus 로고    scopus 로고
    • Native chemical ligation at valine: A contribution to peptide and glycopeptide synthesis
    • Chen, J., Wan, Q., Yuan, Y., Zhu, J., and Danishefsky, S. J. (2008) Native chemical ligation at valine: a contribution to peptide and glycopeptide synthesis. Angew. Chem. Int. Ed. Engl. 47, 8521-8524
    • (2008) Angew. Chem. Int. Ed. Engl. , vol.47 , pp. 8521-8524
    • Chen, J.1    Wan, Q.2    Yuan, Y.3    Zhu, J.4    Danishefsky, S.J.5
  • 43
    • 0343889591 scopus 로고
    • Some synthetic and hydrolytic experiments with chymotrypsin
    • Bergmann, M., and Fruton, J. S. (1938) Some synthetic and hydrolytic experiments with chymotrypsin. J. Biol. Chem. 124, 321-329
    • (1938) J. Biol. Chem. , vol.124 , pp. 321-329
    • Bergmann, M.1    Fruton, J.S.2
  • 44
    • 0030670497 scopus 로고    scopus 로고
    • Synthesis of proteins by subtiligase
    • DOI 10.1016/S0076-6879(97)89053-2
    • Braisted, A. C., Judice, J. K., and Wells, J. A. (1997) Synthesis of proteins by subtiligase. Methods Enzymol. 289, 298-313 (Pubitemid 27467252)
    • (1997) Methods in Enzymology , vol.289 , pp. 298-313
    • Braisted, A.C.1    Judice, J.K.2    Wells, J.A.3
  • 45
    • 8544283771 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of oligosaccharides and glycoproteins
    • DOI 10.1016/j.tibs.2004.10.004, PII S0968000404002695
    • Hanson, S., Best, M., Bryan, M. C., and Wong, C. H. (2004) Chemoenzymatic synthesis of oligosaccharides and glycoproteins. Trends Biochem. Sci. 29, 656-663 (Pubitemid 39491264)
    • (2004) Trends in Biochemical Sciences , vol.29 , Issue.12 , pp. 656-663
    • Hanson, S.1    Best, M.2    Bryan, M.C.3    Wong, C.-H.4
  • 46
    • 0028829779 scopus 로고
    • Enzymic cyclization of linear peptide esters using subtiligase
    • Jackson, D. Y., Burnier, J. P., and Wells, J. A. (1995) Enzymic cyclization of linear peptide esters using subtiligase. J. Am. Chem. Soc. 117, 819-820
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 819-820
    • Jackson, D.Y.1    Burnier, J.P.2    Wells, J.A.3
  • 47
    • 41349093723 scopus 로고    scopus 로고
    • Subtiligase as a hydrothiolase for the synthesis of peptide thioacids
    • Tan, X. H., Yang, R., Wirjo, A., and Liu, C. F. (2008) Subtiligase as a hydrothiolase for the synthesis of peptide thioacids. Tetrahedron Lett. 49, 2891-2894
    • (2008) Tetrahedron Lett. , vol.49 , pp. 2891-2894
    • Tan, X.H.1    Yang, R.2    Wirjo, A.3    Liu, C.F.4
  • 48
    • 0038498076 scopus 로고    scopus 로고
    • Enzymatic cyclization of a potent bowman-birk protease inhibitor, sunflower trypsin inhibitor-1, and solution structure of an acyclic precursor peptide
    • DOI 10.1074/jbc.M212996200
    • Marx, U. C., Korsinczky, M. L., Schirra, H. J., Jones, A., Condie, B., Otvos, L., Jr., and Craik, D. J. (2003) Enzymatic cyclization of a potent Bowman-Birk protease inhibitor, sunflower trypsin inhibitor-1, and solution structure of an acyclic precursor peptide. J. Biol. Chem. 278, 21782-21789 (Pubitemid 36792582)
    • (2003) Journal of Biological Chemistry , vol.278 , Issue.24 , pp. 21782-21789
    • Marx, U.C.1    Korsinczky, M.L.J.2    Schirra, H.J.3    Jones, A.4    Condie, B.5    Otvos Jr., L.6    Craik, D.J.7
  • 49
    • 41549150296 scopus 로고    scopus 로고
    • Chemical and biomimetic total syntheses of natural and engineered MCoTI cyclotides
    • DOI 10.1039/b801667d
    • Thongyoo, P., Roqué-Rosell, N., Leatherbarrow, R. J., and Tate, E. W. (2008) Chemical and biomimetic total syntheses of natural and engineered MCoTI cyclotides. Org. Biomol. Chem. 6, 1462-1470 (Pubitemid 351469865)
    • (2008) Organic and Biomolecular Chemistry , vol.6 , Issue.8 , pp. 1462-1470
    • Thongyoo, P.1    Roque-Rosell, N.2    Leatherbarrow, R.J.3    Tate, E.W.4
  • 51
    • 64549116362 scopus 로고    scopus 로고
    • Dissecting the oxidative folding of circular cystine knot miniproteins
    • Gunasekera, S., Daly, N. L., Clark, R. J., and Craik, D. J. (2009) Dissecting the oxidative folding of circular cystine knot miniproteins. Antioxid. Redox Signal. 11, 971-980
    • (2009) Antioxid. Redox Signal. , vol.11 , pp. 971-980
    • Gunasekera, S.1    Daly, N.L.2    Clark, R.J.3    Craik, D.J.4
  • 52
    • 33745818585 scopus 로고    scopus 로고
    • Oxidative protein folding: Many different ways to introduce disulfide bonds
    • Kadokura, H. (2006) Oxidative protein folding: many different ways to introduce disulfide bonds. Antioxid. Redox Signal. 8, 731-733
    • (2006) Antioxid. Redox Signal. , vol.8 , pp. 731-733
    • Kadokura, H.1
  • 53
    • 33646350007 scopus 로고    scopus 로고
    • Folding of small disulfide-rich proteins: clarifying the puzzle
    • DOI 10.1016/j.tibs.2006.03.005, PII S096800040600082X
    • Arolas, J. L., Aviles, F. X., Chang, J. Y., and Ventura, S. (2006) Folding of small disulfide-rich proteins: clarifying the puzzle. Trends Biochem. Sci. 31, 292-301 (Pubitemid 43674360)
    • (2006) Trends in Biochemical Sciences , vol.31 , Issue.5 , pp. 292-301
    • Arolas, J.L.1    Aviles, F.X.2    Chang, J.-Y.3    Ventura, S.4
  • 54
    • 0033543137 scopus 로고    scopus 로고
    • Chemical synthesis and folding pathways of large cyclic polypeptides: Studies of the cystine knot polypeptide kalata B
    • Daly, N. L., Love, S., Alewood, P. F., and Craik, D. J. (1999) Chemical synthesis and folding pathways of large cyclic polypeptides: studies of the cystine knot polypeptide kalata B. Biochemistry 38, 10606-10614
    • (1999) Biochemistry , vol.38 , pp. 10606-10614
    • Daly, N.L.1    Love, S.2    Alewood, P.F.3    Craik, D.J.4
  • 55
    • 0029904934 scopus 로고    scopus 로고
    • Cyclic peptides from linear unprotected peptide precursors through thiazolidine formation
    • DOI 10.1021/ja954278g, PII S0002786395042788
    • Botti, P., Pallin, T. D., and Tam, J. P. (1996) Cyclic peptides from linear unprotected peptide precursors through thiazolidine formation. J. Am. Chem. Soc. 118, 10018-10024 (Pubitemid 26375185)
    • (1996) Journal of the American Chemical Society , vol.118 , Issue.42 , pp. 10018-10024
    • Botti, P.1    Pallin, T.D.2    Tam, J.P.3
  • 57
    • 34748868370 scopus 로고    scopus 로고
    • Insights from Atomic-Resolution X-Ray Structures of Chemically Synthesized HIV-1 Protease in Complex with Inhibitors
    • DOI 10.1016/j.jmb.2007.07.054, PII S0022283607010078
    • Johnson, E. C., Malito, E., Shen, Y., Pentelute, B., Rich, D., Florián, J., Tang, W. J., and Kent, S. B. (2007) Insights from atomic resolution x-ray structures of chemically synthesized HIV-1 protease in complex with inhibitors. J. Mol. Biol. 373, 573-586 (Pubitemid 47488390)
    • (2007) Journal of Molecular Biology , vol.373 , Issue.3 , pp. 573-586
    • Johnson, E.C.B.1    Malito, E.2    Shen, Y.3    Pentelute, B.4    Rich, D.5    Florian, J.6    Tang, W.-J.7    Kent, S.B.H.8
  • 58
    • 70449636047 scopus 로고    scopus 로고
    • Synthesis of peptide thioesters via an N-S acyl shift reaction under mild acidic conditions on an N-4,5-dimethoxy-2-mercaptobenzyl auxiliary group
    • Nakamura, K., Kanao, T., Uesugi, T., Hara, T., Sato, T., Kawakami, T., and Aimoto, S. (2009) Synthesis of peptide thioesters via an N-S acyl shift reaction under mild acidic conditions on an N-4,5-dimethoxy-2-mercaptobenzyl auxiliary group. J. Pept. Sci. 15, 731-737
    • (2009) J. Pept. Sci. , vol.15 , pp. 731-737
    • Nakamura, K.1    Kanao, T.2    Uesugi, T.3    Hara, T.4    Sato, T.5    Kawakami, T.6    Aimoto, S.7
  • 59
    • 77951174297 scopus 로고    scopus 로고
    • Salicylaldehyde ester-induced chemoselective peptide ligations: Enabling generation of natural peptidic linkages at the serine/threonine sites
    • Li, X., Lam, H. Y., Zhang, Y., and Chan, C. K. (2010) Salicylaldehyde ester-induced chemoselective peptide ligations: enabling generation of natural peptidic linkages at the serine/threonine sites. Org. Lett. 12, 1724-1727
    • (2010) Org. Lett. , vol.12 , pp. 1724-1727
    • Li, X.1    Lam, H.Y.2    Zhang, Y.3    Chan, C.K.4
  • 60
    • 0034643993 scopus 로고    scopus 로고
    • A "traceless"Staudinger ligation for the chemoselective synthesis of amide bonds
    • Saxon, E., Armstrong, J. I., and Bertozzi, C. R. (2000) A "traceless"Staudinger ligation for the chemoselective synthesis of amide bonds. Org. Lett. 2, 2141-2143
    • (2000) Org. Lett. , vol.2 , pp. 2141-2143
    • Saxon, E.1    Armstrong, J.I.2    Bertozzi, C.R.3
  • 61
    • 0034729576 scopus 로고    scopus 로고
    • Staudinger ligation: A peptide from a thioester and azide
    • Nilsson, B. L., Kiessling, L. L., and Raines, R. T. (2000) Staudinger ligation: a peptide from a thioester and azide. Org. Lett. 2, 1939-1941
    • (2000) Org. Lett. , vol.2 , pp. 1939-1941
    • Nilsson, B.L.1    Kiessling, L.L.2    Raines, R.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.